CN85108251A - Decomposition sodium aluminate liquid is made method of alumina and equipment under the no stirring state - Google Patents
Decomposition sodium aluminate liquid is made method of alumina and equipment under the no stirring state Download PDFInfo
- Publication number
- CN85108251A CN85108251A CN85108251.3A CN85108251A CN85108251A CN 85108251 A CN85108251 A CN 85108251A CN 85108251 A CN85108251 A CN 85108251A CN 85108251 A CN85108251 A CN 85108251A
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- China
- Prior art keywords
- suspension
- decomposer
- equipment
- decomposition
- sodium aluminate
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- Expired - Lifetime
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F7/00—Compounds of aluminium
- C01F7/02—Aluminium oxide; Aluminium hydroxide; Aluminates
- C01F7/04—Preparation of alkali metal aluminates; Aluminium oxide or hydroxide therefrom
- C01F7/14—Aluminium oxide or hydroxide from alkali metal aluminates
- C01F7/144—Aluminium oxide or hydroxide from alkali metal aluminates from aqueous aluminate solutions by precipitation due to cooling, e.g. as part of the Bayer process
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F7/00—Compounds of aluminium
- C01F7/02—Aluminium oxide; Aluminium hydroxide; Aluminates
- C01F7/04—Preparation of alkali metal aluminates; Aluminium oxide or hydroxide therefrom
- C01F7/14—Aluminium oxide or hydroxide from alkali metal aluminates
- C01F7/144—Aluminium oxide or hydroxide from alkali metal aluminates from aqueous aluminate solutions by precipitation due to cooling, e.g. as part of the Bayer process
- C01F7/147—Apparatus for precipitation
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/50—Agglomerated particles
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Detergent Compositions (AREA)
Abstract
The present invention relates to decomposition method and its equipment of the sodium aluminate solution of supersaturation alumina.This solution system causes decomposition with alkali and bauxite effect with hibbsite, generates suspension thus.Suspension flows out by the top adding of non-stirring reactor (title decomposer) and by the bottom in this method.The dirty speed setting of suspension is at per hour 1.5 to 10 meters.This device comprises cylinder-cylindroconical reactor, and liquid-adding device is arranged at the top, and the pipe that is contained in decomposer inside is arranged, and the air bottom injection tube is promoted to suspension self-decomposition trench bottom the groove heights of roofs and guides into dirty.
Description
The present invention relates under no stirring state, decompose the method and apparatus of supersaturated sodium aluminate solution, this solution is prepared for Baeyer (Bayer) manufactured aluminum oxide, this is a basic skills of making aluminum oxide, and the aluminum oxide of gained mainly is to be used for high-temperature electrolysis (fused salt electrolysis) production aluminium.According to bayer's process, the aqueous sodium hydroxide solution heat treated of bauxite mine and suitable concn makes it dissolving, makes oversaturated sodium aluminate solution.After not molten slag (red soil) separation, in supersaturated sodium aluminate solution, add some aluminium hydroxide as initiator, just produce aluminum hydroxide precipitation.
This operation, common name " decomposition " generally divides several steps to carry out on technology.The distribution of the main apparent temperature of these steps, granularity and the add-on of initiator, solution carry out mobile and arrange, may also include the layout etc. of recirculation and difference to some extent in a series of groove.
Industrial plants with bayer's process manufacturing aluminum oxide in the world today all are to adopt the stirring-type decomposer, during structurally with use, all to there be preventive measures to avoid stirring and any termination of mobile, otherwise will cause hibbsite to come out at bottom aggradation, this deposition can not reversely be carried out again, so need empty groove and free settling with chemical process.
In fact, be logical with stirring, it can make the aluminium hydroxide suspensoid in the aluminate solution keep in some cases being evenly distributed, and can prevent at decomposer bottom caking.
But need not stir to have several advantages.At first since the reaction under piston pressurized fluid stream condition, carry out, its dynamic performance than the situation that fully stirs into the homogeneous medium for good, so the decomposition rate of aluminate can improve.
Secondly,, strengthened gathering of granule aluminium hydroxide, helped to obtain containing the minimum size-grade distribution of small-particle from the quality viewpoint.
No matter at last, can also see, be that mechanical stirring or produce with injection air stirs, and its energy expenditure all is very important.Stir required power for keeping, concerning the volume of 1000 cubes of meter levels, each trough can reach tens kilowatts (for example 50-55 kilowatt/1000 meters
3).
Except French Patent FR-A-2446799(=CA1117274), also there is not the document record of " bayer's process " supersaturation aluminate solution decomposer that need not stir so far.This French Patent has been narrated a kind of decomposition method that has only gentle agitation, be aluminate solution to be imported the bottom of decomposer with the rotation shower that the perforation side arm is housed, so in the solution that is decomposed not the importing because of solution cause any turbulent flow.Lean solution is discharged from the overflow of decomposer top, and obtains oarse-grained trihydrate disperse phase in the bottom.This process that upwards circulates of aluminate solution can be equal to mutually with the decomposition in the fluidized-bed of gentle agitation, and its application comprises that the low speed of solution circulates.
The present invention is different with traditional concept and industrial practice, and purpose is need not any stirring to handle bauxite and the supersaturated sodium aluminate solution that obtains to decompose with bayer's process.
More particularly, first purpose of the present invention is to propose a kind of method to decompose the sodium aluminate solution that supersaturation alumina is arranged that obtains with alkaline purification bauxite according to bayer's process.Decomposition course is caused by hibbsite, like this, generates the suspension (calling " suspension " in the following text) of hibbsite in sodium aluminate solution.This process is characterised in that suspension is the top importing from the non-stirring reactor that is called " decomposer ", and flows out from the bottom of decomposer.On aluminum oxide industry was produced, the volume of used now decomposer and flow were per hour 1.5 to 19 cubic metres concerning the circulation of suspension, preferably per hour 3 to 7 cubic metres.
Second purpose of the present invention is to arrange to realize the required setting of decomposition course of no any stirring.It is characterized in that it is made up of reactor, the device that imports suspension is arranged at the top of this reactor, and the bottom is furnished with the device that takes out suspension, and reactor is garden post-taper, and the device that takes out suspension is connected in the summit neighbour of tapered section.
The device that takes out aluminate suspension is a pipe, and by its bottom injecting compressed air, gas outlet chamber is equipped with at the top, and gas outlet chamber is connected in pipeline and the recirculation overflow port that leads to next trough.
Fig. 1 and Fig. 2 are the diagrammatic elevational view of equipment of the present invention.
Fig. 1 is a decomposer that need not any stirring of the present invention, and Fig. 2 is improved equipment.
Decomposer (1) is garden post-taper, is made up of the top (2) and the taper bottom (3) of garden cylindricality.The pipe (4) of a band piston did not drink up suspension at the end of cone.The device (5) that injecting compressed air is arranged in the pipe (4) makes the upstanding portion at pipe (4) form the emulsification post.Emulsive hydrated aluminum oxide suspension rises and enters gas outlet chamber (6) and the transport pipe (7) in order to be full of the downstream.Is furnished with a stopping valve (8) on the pipeline (7).Gas outlet chamber (6) also has an overflow port (9), allows overflow liquid flow back to decomposer.
The flow velocity of the suspension that is transferred changes because of the air velocity of pipe (5).The flow velocity of air is regulated by the liquid level of groove.At this moment the auxiliary adjustment of fixed air velocity can prevent that air injection tube is blocked and make the amount of liquid of conveying more even.The fixed flow rate of air is by valve (10) control, and remote valve (11) is a flow velocity of regulating air according to the liquid level of aluminate suspension in the decomposer.
In a single day the solution of non-stirring decomposer supplied with and finished, and the valve (8) on the transport pipe (7) cuts out automatically, and the pressure lock (12) in parallel with two above-mentioned valves (also being remote control) opened simultaneously.The breakdown of valve has increased the injection rate of air, allow the overflow port (9) of suspension by gas outlet chamber (6) top again internal recycling in groove, prevented the accumulation of solid thus at bottom land.A main cut-off valve (13) at least also will be arranged on the loop.
Preferably use decollator to make it even from last trough via the hibbsite suspension that pipeline (14) stream comes in decomposer (18) surface arrangement as (15), decollator can be the tilting tubule (16) in a series of immersion solution, in its bottom the pressurized air thread of sending here from pipe (17) is arranged, they play a part emulsor, perhaps also can be with known suitable device on any technology.
Suspension among Fig. 2 is the bottom of taking from cone (3), makes it upwards with air lance (5) or pump (19) by outer tube.In all cases, tubing system and the following current pipe (7) that is back to groove (1) is equipped with at the top of pipe (4), and pipe (7) is equipped with a stopping valve (8) at least.
In bayer's process, sodium aluminate solution is normally used causticity Na wherein
2The concentration of O and weight ratio WR determine that weight ratio is aluminum oxide (Al
2O
3) the weight of weight ratio caustic soda.Caustic soda is with the Na in the sodium aluminate solution that is decomposed
2The combined form of O(in sodium aluminate and the free state form of sodium hydroxide) total amount represents.
Enter the suspension of first decomposer, its weight ratio is about 1.05 to 1.10, causticity Na
2The content of O is about every liter 150 to 160 gram.
This decomposer that feeds in raw material, extracts in the bottom suspension at upper surface is hydraulically operated, and liquid stream slowly is referred to as " piston flow ".This stream of liquid does not slowly cause any stirring, thereby can set up stable dynamic equilibrium in groove.
In equilibrium state, constant weight ratio (but there is different numerical value in each cross section) is arranged all on each horizontal section of solution.Lower horizontal cross section weight ratio increases, and simultaneously, each side still is in close proximity to the theoretical dynamic performance of common discontinuous decomposition (so-called rhythmic reaction).
Example
1. in the full scale plant of first example, two placed in-line decomposers are arranged, operational condition is as follows:
The feature of each decomposer:
Volume=1250 meter
3
Height=17 of garden post part meter
The height of garden wimble fraction=9 meter, 60 ℃ of taperings
Horizontal section=63 meter
2
The feature of suspension:
Every liter contains 150 gram caustic sodas in the sodium aluminate
Dry-matter=720 grams per liters
Granular size D
50=45 microns
Temperature=60 ℃
Hydromeehanics and chemical feature:
First decomposer: flow=430 meter
3/ hour
Speed=6.8 meter/hour
The WR(import)=1.03
The WR(outlet)=0.89
On-stream period=4 that twice chemical process freed to transport between the settling month
(the similar decomposer running that band stirs three months).
Second decomposer: flow=215 meter
3/ hour
Speed=3.4 meter/hour
The WR(import)=0.89
The WR(outlet)=0.78
On-stream period＞5 that twice chemical process freed to transport between the settling month
(similar stirring decomposer running 4 months).
[stir the WR(outlet of decomposer) be 0.82].
2. the full scale plant of second example is a decomposer, and operational condition is as follows:
The decomposer feature:
Volume=3000 meter
3
Height=24 meter of part are leant in the garden
The height of garden wimble fraction=10 meter
Horizontal section=113.5 meter
2
The suspension feature:
Every liter contains 165 gram caustic sodas in the sodium aluminate
Dry-matter=650 grams per liters
Granular size D
50=80 microns
Temperature=60 ℃
Hydrodynamics characteristic:
Speed=3.1 meter/hour
Flow=350 meter
3/ hour
The WR(import)=0.95
The WR(outlet)=0.82
The benefit of gained of the present invention
A) the energy benefit is as above-mentioned. With the stirring decomposer of air floatation, stirring needs tens kilowatts of electric power, and the air that emulsification is used needs every minute tens standard cubic meters. By the present invention, all agitation energy are equal Can save, and the required air consumption of suspension 1 to 2 standard cubic meter that can reduce to every minute in the increased pipe (4). The cost that this kind groove is installed is more much lower than tank diameter is installed.
B) operation and maintenance of this method is much easier than stirring decomposer.
Its bottom land non flouling behaviour of non-stirring decomposer. The deposition that generates in deposition on the cell wall and the tank diameter is identical.
The adjusting of liquid level is easy especially, and the air that enters pipe (4) regulated by a need and the phegma that passes through overflow port gets final product, and especially the supply at suspension has fluctuation, when perhaps even fully stopping.When general power failure,, avoided non-reversibility deposition at bottom land as long as there is a little compressed air require just enough to keep the backflow of liquid.And carry out in the emulsive decomposer in mechanical stirring or with a large amount of pressurized air, this outage is catastrophic often.
C) from method itself, for the carrying out of reaction, in no any stirring with under a direction mobile situation, the volume of decomposer can utilize better, and its reason is as follows:
1. do not have the dead band in the groove, all available volumes have all utilized.In adopting the conventional steel basin of air floatation, the volume of air that generates emulsion reach groove cubic capacity 10 to 15%.
2. owing to be piston flow, reaction is clocklike, and is unruffled.
Because these reasons are so the present invention has done the improvement of highly significant on the continuous production method of alumina of bayer's process.
Claims (13)
1, the decomposition method of the oversaturated sodium aluminate solution of a kind of aluminum oxide, this sodium aluminate solution system makes with alkali and bauxite effect by bayer's process, decomposition is to be caused by hibbsite, and generation suspension, it is characterized in that suspension is imported by the non-stirred reactor top that is called " decomposer " and takes out from the bottom.
2,, it is characterized in that the velocity of flow of suspension is to be adjusted in per hour 1.5 to 10 meters in the decomposer according to the method for claim 1.
3,, it is characterized in that the velocity of flow of suspension in the decomposer preferably is adjusted to per hour 3 to 7 meters according to the method for claim 1.
4,, it is characterized in that suspension is it is dispersed in whole surface makes it basically uniformly that device imports from the top of decomposer with a kind of according to the method for claim 1.
5, according to the method for claim 1, it is characterized in that suspension is to be contained in the pipe in the groove from the bottom of decomposer by one and to inject the top liquid level that air makes suspension rise to decomposer in its underpart and discharge, and fed downstream thus.
6,, it is characterized in that suspension is to make suspension rise to the liquid level equal-height position of decomposer, fed downstream then from the bottom of decomposer by the pipe outside the groove according to the method for claim 1.
7, according to each equipment for realization nothing stirring decomposition course of claim 1 to 6, it is characterized in that it is a reactive tank, the groove top is furnished with the device of the importing suspension as (14), and trench bottom is equipped with the device (4) that takes out suspension.
8, according to the equipment of claim 7, it is characterized in that reactive tank (1) is garden post-taper, the device that takes out aluminate suspension is connected the vertex of a cone nearby.
9, equipment according to Claim 8, it is characterized in that: the device that takes out aluminate suspension is a pipe (4), the device (5) of injecting compressed air is arranged at its bottom, and gas outlet chamber (6) is equipped with at the top, and gas outlet chamber links to each other with backflow overflow port (9) with dirty transfer lime (7).
10, according to the equipment of claim 7, it is characterized in that it includes device as (15), be used for dispersion suspension liquid, make on whole decomposer surface (18) uniform distribution basically.
11, according to the equipment of claim 10, it is characterized in that diverting device (15) is made up of many tipping tubes (16) that are contained in decomposer (1) top and immerse in the solution, compressed-air actuated thread ejection is arranged in the bottom of these tipping tubes.
12,, it is characterized in that it includes injection tube (4) checked and regulated by a cover according to the liquid level of suspension in the decomposer compressed-air actuated device according to the equipment of claim 7.
13, each equipment in 11 according to Claim 8 is characterized in that it includes injection tube (4) checked and regulated by a cover according to the liquid level of suspension in the decomposer compressed-air actuated device.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8504598 | 1985-03-20 | ||
| FR8504598A FR2579194B1 (en) | 1985-03-20 | 1985-03-20 | PROCESS AND DEVICE WITHOUT AGITATION OF SODIUM ALUMINATE LIQUORS FOR THE PRODUCTION OF ALUMINA |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN85108251A true CN85108251A (en) | 1986-09-17 |
| CN1003368B CN1003368B (en) | 1989-02-22 |
Family
ID=9317654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN85108251.3A Expired CN1003368B (en) | 1985-03-20 | 1985-11-13 | Method and apparatus for alumina prepn. by decomposing sodium aluminate solution without stirring |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US4666687A (en) |
| EP (1) | EP0195732B1 (en) |
| JP (1) | JPS61215213A (en) |
| CN (1) | CN1003368B (en) |
| AU (1) | AU579921B2 (en) |
| BR (1) | BR8601223A (en) |
| CA (1) | CA1281885C (en) |
| DE (1) | DE3666580D1 (en) |
| ES (1) | ES8800116A1 (en) |
| FR (1) | FR2579194B1 (en) |
| GB (2) | GB2172587B (en) |
| GR (1) | GR860723B (en) |
| HU (1) | HU199083B (en) |
| IE (1) | IE58878B1 (en) |
| IN (1) | IN167095B (en) |
| NO (1) | NO172040C (en) |
| OA (1) | OA08268A (en) |
| YU (2) | YU44117B (en) |
| ZA (1) | ZA862036B (en) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2598701B1 (en) * | 1986-05-15 | 1988-08-05 | Pechiney Aluminium | PROCESS AND DEVICE FOR DECOMPOSING SODIUM ALUMINATE LIQUOR FOR THE PRODUCTION OF ALUMINA |
| US4847064A (en) * | 1987-12-23 | 1989-07-11 | Aluminum Company Of America | Economical process for alpha alumina production |
| US5225229A (en) * | 1986-07-18 | 1993-07-06 | Aluminum Company Of America | Aluminum hydroxide production |
| GR1001384B (en) * | 1990-01-04 | 1993-10-29 | Vni I Pi Aljuminievo | Arrangement for slump pots |
| US5122348A (en) * | 1991-01-09 | 1992-06-16 | Alcan International Limited | Method of slurrying partially calcined alumina dust |
| US5249861A (en) * | 1991-07-18 | 1993-10-05 | Kusel Equipment Co. | Apparatus for cooling, washing, draining, and blending liquid suspended materials |
| AU650199B1 (en) * | 1992-08-03 | 1994-06-09 | Nalco Chemical Company | Method for the alteration of siliceous materials from Bayer process liquors |
| TW479841U (en) * | 1998-06-17 | 2002-03-11 | United Microelectronics Corp | Polishing slurry supply apparatus |
| US6713428B1 (en) † | 1998-07-06 | 2004-03-30 | Instuit Francais Du Petrole | Dispersible aluminium hydrate, method for preparing same and use for preparing catalysts |
| US7731411B2 (en) * | 2005-04-04 | 2010-06-08 | Schlumberger Technology Corporation | Circulating fluid system for powder fluidization and method of performing same |
| US7785479B1 (en) * | 2007-05-01 | 2010-08-31 | Michael Hays Hosford | Apparatus and method of separating |
| KR101235123B1 (en) * | 2011-07-15 | 2013-02-20 | 주식회사제오빌더 | Process for preparing porous alumina |
| RU2614717C1 (en) * | 2015-11-13 | 2017-03-28 | Общество с ограниченной ответственностью "Объединенная Компания РУСАЛ Инженерно-технологический центр" | Carbonizer |
| WO2017223269A1 (en) | 2016-06-24 | 2017-12-28 | Lonza Ltd. | Variable diameter bioreactors |
| CN111634932B (en) * | 2020-05-28 | 2022-08-05 | 中国铝业股份有限公司 | System for continuously producing pseudo-boehmite and use method thereof |
| RU2756211C1 (en) * | 2020-12-01 | 2021-09-28 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Красноярский государственный аграрный университет" | Carbonizer |
| CN112546946B (en) * | 2020-12-08 | 2021-08-13 | 山东瑞尚机械有限公司 | Aluminum oxide seed precipitation decomposer |
| CN113149049A (en) * | 2021-05-13 | 2021-07-23 | 云南文山铝业有限公司 | Grader mother liquor adding self-pressing device and using method thereof |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1073878A (en) * | 1912-01-20 | 1913-09-23 | Walter E Trent | Agitating and mixing apparatus. |
| DE311368C (en) * | 1912-11-22 | |||
| GB653741A (en) * | 1947-09-25 | 1951-05-23 | Viggo Harms | Improvements in and relating to a method and apparatus for precipitation of solids from solutions and the like |
| US2786722A (en) * | 1951-06-12 | 1957-03-26 | Houdry Process Corp | Disengaging solids from lift gas |
| FR1178685A (en) * | 1957-07-08 | 1959-05-13 | Olin Mathieson | Method and device for crystallization from supersaturated liquid solutions |
| GB996195A (en) * | 1961-08-03 | 1965-06-23 | Aero Hydraulics Ltd | Improvements in methods and apparatus for mixing and dispersing substances and for maintaining dispersions and emulsions |
| CH412811A (en) * | 1962-11-06 | 1966-05-15 | Ruetschi Ag Pumpenbau K | Method of mixing and device for carrying out the method |
| US3372985A (en) * | 1963-02-20 | 1968-03-12 | Kaiser Aluminium Chem Corp | Process for removing impurities from the precipitation system of the bayer process |
| US3351326A (en) * | 1964-10-07 | 1967-11-07 | Rexall Drug Chemical | Process and apparatus for solids blending |
| US3649184A (en) * | 1969-05-29 | 1972-03-14 | Reynolds Metals Co | Precipitation of alumina hydrate |
| JPS504745U (en) * | 1973-05-09 | 1975-01-18 | ||
| US3953003A (en) * | 1974-06-06 | 1976-04-27 | Aluterv Aluminiumipari Tervezo Vallalat | Tank provided with pneumatic mixing pipe |
| US4014985A (en) * | 1975-12-22 | 1977-03-29 | Aluminum Company Of America | Precipitation of aluminum oxide having low sodium oxide content |
| US4530699A (en) * | 1979-01-18 | 1985-07-23 | Aluminum Company Of America | Dense phase precipitation |
| US4370418A (en) * | 1981-07-24 | 1983-01-25 | University Of California | Liquid level control by subsurface draw off |
| DE3269635D1 (en) * | 1982-09-02 | 1986-04-10 | Alcoa Chemie Gmbh | Process for the production of alumine |
| HU193892B (en) * | 1984-02-28 | 1987-12-28 | Magyar Aluminium | Method and apparatus for economical operating pneumatic pulp-mixing reservoirs of mammoth tube |
| HUH3410A (en) * | 1989-10-03 | 1990-03-28 | Arpad Klatsmanyi | Method and circuit arrangement for realizing digital transmission of variable characteristic |
-
1985
- 1985-03-20 FR FR8504598A patent/FR2579194B1/en not_active Expired - Lifetime
- 1985-11-13 CN CN85108251.3A patent/CN1003368B/en not_active Expired
-
1986
- 1986-02-20 US US06/831,269 patent/US4666687A/en not_active Expired - Fee Related
- 1986-03-14 IN IN183/MAS/86A patent/IN167095B/en unknown
- 1986-03-17 EP EP86420076A patent/EP0195732B1/en not_active Expired
- 1986-03-17 DE DE8686420076T patent/DE3666580D1/en not_active Expired
- 1986-03-17 JP JP61059075A patent/JPS61215213A/en active Granted
- 1986-03-17 GB GB8606511A patent/GB2172587B/en not_active Expired
- 1986-03-18 ES ES553103A patent/ES8800116A1/en not_active Expired
- 1986-03-18 GR GR860723A patent/GR860723B/en unknown
- 1986-03-18 CA CA000504350A patent/CA1281885C/en not_active Expired - Fee Related
- 1986-03-19 YU YU436/86A patent/YU44117B/en unknown
- 1986-03-19 HU HU861155A patent/HU199083B/en unknown
- 1986-03-19 BR BR8601223A patent/BR8601223A/en not_active IP Right Cessation
- 1986-03-19 ZA ZA862036A patent/ZA862036B/en unknown
- 1986-03-19 AU AU54906/86A patent/AU579921B2/en not_active Expired
- 1986-03-19 NO NO861070A patent/NO172040C/en unknown
- 1986-03-19 IE IE70586A patent/IE58878B1/en not_active IP Right Cessation
- 1986-03-19 OA OA58815A patent/OA08268A/en unknown
-
1987
- 1987-01-13 US US07/003,046 patent/US4762684A/en not_active Expired - Fee Related
-
1988
- 1988-02-29 YU YU395/88A patent/YU44652B/en unknown
- 1988-04-26 GB GB8809811A patent/GB2203422B/en not_active Expired
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